RS71428908 SCN9A
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What This Variant Does
"CLNSIG=255
Associated Conditions
6 conditions
Neuropathy
hereditary sensory and autonomic
type 2A
Generalized epilepsy with febrile seizures plus
type 7
Primary erythromelalgia
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Paroxysmal extreme pain disorder
Inborn genetic diseases
6 conditions
Neuropathy
hereditary sensory and autonomic
type 2A
Other Variants in SCN9A